Reaktion #532097
ord-c3fc454887404730b2acc39214a39a57
Reaktionsgleichung
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Sonstigeto give a dark brown solution
- 2Temperaturthe mixture was heated
- 3Temperaturat reflux for 4.5 hours
- 4SonstigeThe reaction mixture was quenched
- 5workup.ADDITIONby pouring into vigorously stirring water (600 ml)
- 6workup.ADDITIONcontaining sodium hydrogencarbonate (110 g)
- 7ExtraktionThe dark brown mixture was extracted with DCM (3×200 ml)
- 8Waschenthe organic phase was washed with water (200 ml) and brine (100 ml)
- 9Trocknendried (MgSO4)
- 10Einengenconcentrated in vacuo
Vorschrift
3-Nitro-5-(trifluoromethyl)pyridin-2-ol (31.00 g, 149 mmol) was dissolved in acetonitrile (250 ml) to give a dark brown solution. Phosphorus(V) oxybromide (85 g, 298 mmol) was added and the mixture was heated at reflux for 4.5 hours and then stirred at RT overnight. The reaction mixture was quenched by pouring into vigorously stirring water (600 ml) containing sodium hydrogencarbonate (110 g). The dark brown mixture was extracted with DCM (3×200 ml) and the organic phase was washed with water (200 ml) and brine (100 ml), dried (MgSO4) and concentrated in vacuo to afford the title product as a brown oil. 1H-NMR: [400 MHz, CDCl3, δH, 8.87 (1H, d, J=1.4 Hz, ArH), 8.39 (1H, d, J=1.9 Hz, ArH).